Hyponatremia Clinical Trial
Official title:
Factors Associated With Hyponatremia Induced by High-dose Cyclophosphamide: Prospective Cohort Study
Prospoctive cohort of high-dose cyclophosphamide exposed patients. With active estandardize screening of hyponatremia development in the follow up period.
Primary objectives
1. To identify the factors associated with the development of hyponatremia in patients
receiving high-dose cyclophosphamide (2.5 grams or more).
2. Generate and validate a predictive score of developing hyponatremia high-dose
cyclophosphamide.
3. To estimate the incidence of hyponatremia in patients undergoing high-dose
cyclophosphamide.
Study design. Observational prospective cohort study of Patients after infusion of high-dose
cyclophosphamide. Follow up period will be from cyclophosphamide infusion until one month
after hospital discharge.
;
Observational Model: Cohort, Time Perspective: Prospective
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